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Sigma-Aldrich

Methylamine-13C hydrochloride

99 atom % 13C

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250 MG
$324.00
1 G
$705.00

$324.00


Available to ship onMay 01, 2025Details


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250 MG
$324.00
1 G
$705.00

About This Item

Linear Formula:
13CH3NH2 · HCl
CAS Number:
Molecular Weight:
68.51
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.12

$324.00


Available to ship onMay 01, 2025Details


Request more information

isotopic purity

99 atom % 13C

Quality Level

form

solid

technique(s)

protein expression: suitable

mp

232-234 °C (lit.)

mass shift

M+1

SMILES string

Cl.[13CH3]N

InChI

1S/CH5N.ClH/c1-2;/h2H2,1H3;1H/i1+1;

InChI key

NQMRYBIKMRVZLB-YTBWXGASSA-N

Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

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signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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Nicolas Fleury-Brégeot et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(31), 9564-9570 (2012-07-07)
Ammoniomethyl trifluoroborates are very powerful reagents that can be used to access biologically relevant aryl- and heteroaryl-methylamine motifs via Suzuki-Miyaura cross-couplings. Until now, this method was limited to the production of tertiary and primary amines. The synthesis of a large
Sucismita Chutia et al.
The journal of physical chemistry. B, 116(51), 14788-14804 (2012-11-23)
We study the initial steps of the interaction of water molecules with two unsolvated peptides: Ac-Ala(5)-LysH(+) and Ac-Ala(8)-LysH(+). Each peptide has two primary candidate sites for water adsorption near the C-terminus: a protonated carboxyl group and the protonated ammonium group
Chaehyuk Ko et al.
The journal of physical chemistry. B, 117(1), 316-325 (2012-12-15)
Proton-coupled electron transfer can occur through concerted (electron-proton transfer, EPT) or sequential mechanisms, but this distinction becomes less well-defined for photoinduced reactions. These issues have been examined with transient absorption experiments on a hydrogen-bonded complex consisting of p-nitrophenylphenol and t-butylamine.

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